Hair AF

Manufacturer: GC Love LLC
Effective date: 2021-10-22
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:15:08

Label at a glance#

ProductHair AF

Active ingredientBETULA PUBESCENS FLOWER BUD, CASTANEA SATIVA LEAF, HUMAN HAIR, PHOSPHORUS, POPULUS NIGRA LEAF BUD, SACCHAROMYCES CEREVISIAE RNA

Label structure9 sections

Indications and uses

For temporary relief of minor: hair loss Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. itchy scalp scaliness of scalp

Dosage and administration

Adults: Take 10 drops under the tongue 3 times a day, or as directed by your healthcare professional.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients
Betula Pubescens Flower Bud	2X
Castanea Vesca	2X
Human Hair	4C 7C
Phosphorus	5X 6X 8X 12X 3C 5C 6C 7C
Populus Nigra Leaf Bud	2X
RNA	3x 4x

Uses

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

For temporary relief of minor:

hair loss¹
itchy scalp¹
scaliness of scalp¹

1 Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Warnings

WARNINGS SECTION

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use. Do not use if clear seal over the cap is broken or missing.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if hair loss, itchy scalp, scaliness of scalp, or other symptoms do not improve within 7 days or are accompanied by fever.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults: Take 10 drops under the tongue 3 times a day, or as directed by your healthcare professional.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

alcohol (20% by volume), distilled water

Questions?

OTC - QUESTIONS SECTION

27510 Ave Mentry, Valencia, CA 91355, USA

SPL UNCLASSIFIED SECTION

Distributed by GC Love, LLC.

PRINCIPAL DISPLAY PANEL - 60 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GC
LOVE™

Hair AF™
Homeopathic Formula

Hair Loss*

2 fl oz (60 mL)
Alcohol 20% by Volume

Principal Display Panel - 60 mL Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
81812-0101-1	2024-01-30	C162847	48780-1	1030e365-6dac-111a-e063-dadaa90a10e2	Hair AF™

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
81812-0101-1	Hair AF	60 mL in 1 BOTTLE, GLASS	SOLUTION	60		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
81812-0101	HAIR AF (BETULA PUBESCENS FLOWER BUD, CASTANEA SATIVA LEAF, HUMAN HAIR, PHOSPHORUS, POPULUS NIGRA LEAF BUD, AND SACCHAROMYCES CEREVISIAE RNA) SOLUTION [GC LOVE LLC]	2	Legacy NDC, 1 package rows	20211102_7b05cb41-b143-4639-9e94-fc5bd1fe6195.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

Hair AF
betula pubescens flower bud, castanea sativa leaf, human hair, phosphorus, populus nigra leaf bud, and saccharomyces cerevisiae rna
BETULA PUBESCENS FLOWER BUD
CASTANEA SATIVA LEAF
HUMAN HAIR
PHOSPHORUS
POPULUS NIGRA LEAF BUD
SACCHAROMYCES CEREVISIAE RNA
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
81812-0101	81812-0101-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BETULA PUBESCENS FLOWER BUD	32JS91VU1G	ACTIB
CASTANEA SATIVA LEAF	IV3S2HH53G	ACTIB
HUMAN HAIR	1AWP0DKL4I	ACTIB
PHOSPHORUS	27YLU75U4W	ACTIB
POPULUS NIGRA LEAF BUD	GJU5F9OXMT	ACTIB
SACCHAROMYCES CEREVISIAE RNA	J17GBZ5VGX	ACTIB
ALCOHOL	3K9958V90M	IACT
WATER	059QF0KO0R	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
65c05bd5-cd33-4e42-8278-e5940c4d831d			7b05cb41-b143-4639-9e94-fc5bd1fe6195	2021-10-22	Warnings	Exact identifier spl id: 65c05bd5-cd33-4e42-8278-e5940c4d831d spl set id: 7b05cb41-b143-4639-9e94-fc5bd1fe6195

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.